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Lead Validation Specialist – GMP CSV
Descripción de la vacante
A cell and gene therapy company in Scotland is seeking a Validation Supervisor to supervise a team involved in Computer System Validation (CSV). The role includes overseeing quality documentation, monitoring project milestones, and providing expertise during audits. Applicants should have a degree in Life Sciences or Computer Science and experience in a GMP environment. This is an exciting opportunity to make a significant impact in a rapidly expanding company.
Servicios
Formación
- Proven experience in Computer System Validation within a GMP regulated environment.
- Previous background in supervising or leading teams.
- Demonstrable experience of project‑based work, including regulatory audits.
Responsabilidades
- Supervise a team undertaking CSV activities for the business.
- Complete quality related documentation in accordance with GMP and SOPs.
- Monitor and report on key milestones within CSV projects.
Conocimientos
Educación
* El índice de referencia salarialse calcula en base a los salarios que ofrecen los líderes de mercado en los correspondientes sectores. Su función es guiar a los miembros Prémium a la hora de evaluar las distintas ofertas disponibles y de negociar el sueldo. El índice de referencia no es el salario indicado directamente por la empresa en particular, que podría ser muy superior o inferior.